Synthesis of 5‐Aryltetrahydrobenzazepines
ABSTRACT Envisaging 5‐aryltetrahydrobenzazepinone and 5‐aryltetrahydrobenzazepines as conformationally locked potential B 0 AT1 inhibitors, a convenient synthetic route has been developed for their access. The synthetic route banks on using the Schmidt reaction for quick access to symmetrical/unsymmetrical 5‐aryltetrahydrobenzazepinone and 5‐aryltetrahydrobenzazepines.
Authors
- Indrapal Singh Aidhen (ORCID: https://orcid.org/0000-0002-7330-7404)
- Deepika Gupta (ORCID: https://orcid.org/0000-0002-1353-0057)
- H. B. Lal (ORCID: https://orcid.org/0000-0002-1651-9013)
- Naveenkumar Thoti
Institutions
- Indian Institute of Technology Madras (IN)
Publication Details
- Journal
- Journal of Heterocyclic Chemistry
- Published
- 2024-11-24
- DOI
- https://doi.org/10.1002/jhet.4932
- Citations
- 1
- Primary Topic
- Amino Acid Enzymes and Metabolism
- Type
- article
- Field-Weighted Citation Impact
- 0.29
Funders
- Council of Scientific and Industrial Research, India